1-[(methylcarbamoyl)amino]-1-oxopropan-2-yl4-[(4-methyl-2-oxo-2h-chromen-7-yl)oxy]methylbenzoate

95%

Reagent Code: #213357
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CAS Number 937891-74-2

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 438.43 g/mol
Formula C₂₃H₂₂N₂O₇
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a photolabile protecting group in organic synthesis, particularly in the controlled release of carboxylic acids and alcohols upon exposure to light. Its coumarin-derived core enables efficient cleavage under mild UV irradiation, making it valuable in solid-phase synthesis, peptide chemistry, and drug delivery systems where temporal and spatial control of molecular release is required. Commonly applied in the design of caged compounds for biological studies and in phototriggered prodrug activation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,280.00
inventory 1g
10-20 days ฿27,890.00
1-[(methylcarbamoyl)amino]-1-oxopropan-2-yl4-[(4-methyl-2-oxo-2h-chromen-7-yl)oxy]methylbenzoate
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Used as a photolabile protecting group in organic synthesis, particularly in the controlled release of carboxylic acids and alcohols upon exposure to light. Its coumarin-derived core enables efficient cleavage under mild UV irradiation, making it valuable in solid-phase synthesis, peptide chemistry, and drug delivery systems where temporal and spatial control of molecular release is required. Commonly applied in the design of caged compounds for biological studies and in phototriggered prodrug activation

Used as a photolabile protecting group in organic synthesis, particularly in the controlled release of carboxylic acids and alcohols upon exposure to light. Its coumarin-derived core enables efficient cleavage under mild UV irradiation, making it valuable in solid-phase synthesis, peptide chemistry, and drug delivery systems where temporal and spatial control of molecular release is required. Commonly applied in the design of caged compounds for biological studies and in phototriggered prodrug activation.

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